EZ Smart Stand S400PS1-03Recalls & reported problems
EZ Way, Inc. · 400 lb. Smart Stand® with scale, Standard · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848914000149), received between Mar 24, 2026 and Mar 24, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Bone Fracture(s)1
- Limb Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 24, 2026Insufficient Device Problem Information
RESIDENT WAS USING COMMODE. THE AIDE GOT THE RESIDENT HOOKED UP TO THE STAND AND SHE CHECKED HIS FEET AND HANDS BEFORE LIFTING. THE STAND STOPPED ON ITS OWN ABOUT HALFWAY UP. THE CNA DID PERI CARE FOR THE RESIDENT. THE STAND WOULD NOT GO ALL THE WAY UP, SO THE CNA GOT A WHEELCHAIR TO LOWER THE RESIDENT ONTO. BEFORE SHE COULD DO SO, THE RESDIENT SAID HE WAS GOING DOWN. HE WASN'T ABLE TO HANG ONTO THE HANDLE GRIPS. THE CNA HELPED THE RESIDENT TO THE FLOOR. THE RESIDENT SAID HE HEARD A POP OR SNAP SOUND. THE RESIDENT REFUSED TO GO TO THE ER THAT DAY. THE NEXT DAY, THERE WERE VISIBLE SIGNS OF INJURIES ON THE RESIDENT. HE WENT TO ER THE FOLLOWING MORNING AND WAS IN 10 OUT OF 10 FOR PAIN. HE HAD SURGERY DONE ON HIS LEG FOR A BROKEN FEMUR.
Patient problems: Bone Fracture(s); Limb Fracture
MAUDE report 24675722 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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